A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418607



Internal ID21076160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43005281..43006081hg38UCSC Ensembl
chr8:42860424..42861224hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167608
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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